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Tycheseal™

by Beijing Percutek Therapeutics Inc. 510 variants

Ref PTBS4646150Model PTBS

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06957485024363 Basic UDI-DI 06957485024363UDI-DIDate23 Jun 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Tycheseal™ Thoracic stent graft system
Model / Reference
PTBS, PTBS4646150
Primary DI / UDI-DI
06957485024363
Basic UDI-DI
B-06957485024363
EMDN Code
P070401010102 Dacron vascular endoprostheses, straight - thoracic
Device Class
Class III
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
CN-MF-000013927
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Other devices from Beijing Percutek Therapeutics Inc.

See all devices from Beijing Percutek Therapeutics Inc. →

Properties

  • Sterile

Other properties (12)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No